Anderson Tara L, Morris Jonathan M, Wald John T, Kotsenas Amy L
1 Department of Radiology, Mayo Clinic, 200 First St SW, Rochester, MN 55905.
AJR Am J Roentgenol. 2017 Sep;209(3):648-655. doi: 10.2214/AJR.16.16704. Epub 2017 Jun 22.
Chronic adhesive arachnoiditis (CAA) is rare and has potentially devastating clinical consequences. The objective of this article is to review the clinical features of CAA and describe its appearance on imaging, to increase radiologists' awareness of this challenging diagnosis.
Twenty-nine cases of advanced CAA seen at our institution over 18 years (1995-2013) were retrospectively reviewed. Chart review was performed, with attention given to data on clinical presentation, suspected cause, and interventions performed. All patients underwent MRI, and seven patients also underwent CT myelography. Clinical and imaging features were evaluated and categorized.
The 29 patients ranged in age from 23 to 96 years and included 11 women and 18 men. Suspected underlying causative factors included trauma (n = 10), prior surgery (n = 9), nontraumatic subarachnoid hemorrhage (n = 7), infection (n = 3), myelography with iophendylate used as contrast medium (n = 1), Guillain-Barré syndrome (n = 1), ankylosing spondylitis (n = 1), and unknown causes (n = 1). Imaging characteristics include loculated CSF collections (n = 23), nerve root clumping, enhancement, and displacement (n = 15), cord swelling with increased T2 signal (n = 12), arachnoid septations (n = 11), cord atrophy (n = 6), syrinx (n = 5), and intrathecal calcifications (n = 3). Ten patients underwent surgical procedures, and most had only brief clinical improvement.
CAA is a rare cause of devastating neurologic symptoms and chronic pain. The imaging features of CAA range from subtle to severe. Advanced arachnoiditis can present with spinal cord swelling and syrinx formation, which can mimic other disease processes. Inclusion of advanced CAA in the differential diagnosis can prevent unnecessary interventions.
慢性粘连性蛛网膜炎(CAA)较为罕见,具有潜在的严重临床后果。本文旨在回顾CAA的临床特征并描述其影像学表现,以提高放射科医生对这一具有挑战性诊断的认识。
回顾性分析1995年至2013年18年间在我院就诊的29例晚期CAA病例。进行病历审查,关注临床表现、可疑病因及所采取的干预措施等数据。所有患者均接受了磁共振成像(MRI)检查,7例患者还接受了CT脊髓造影检查。对临床和影像学特征进行评估并分类。
29例患者年龄在23岁至96岁之间,其中女性11例,男性18例。可疑的潜在病因包括创伤(10例)、既往手术(9例)、非创伤性蛛网膜下腔出血(7例)、感染(3例)、使用碘苯酯作为造影剂的脊髓造影(1例)、格林-巴利综合征(1例)、强直性脊柱炎(1例)及病因不明(1例)。影像学特征包括局限性脑脊液积聚(23例)、神经根聚集、强化及移位(15例)、脊髓肿胀伴T2信号增高(12例)、蛛网膜分隔(11例)、脊髓萎缩(6例)、空洞形成(5例)及鞘内钙化(3例)。10例患者接受了手术治疗,多数患者临床症状仅短暂改善。
CAA是导致严重神经症状和慢性疼痛的罕见病因。CAA的影像学特征范围从轻微到严重。晚期蛛网膜炎可表现为脊髓肿胀和空洞形成,可模仿其他疾病过程。在鉴别诊断中考虑晚期CAA可避免不必要的干预。